期刊
METALLURGICAL AND MATERIALS TRANSACTIONS A-PHYSICAL METALLURGY AND MATERIALS SCIENCE
卷 45A, 期 3, 页码 1247-1257出版社
SPRINGER
DOI: 10.1007/s11661-013-2053-8
关键词
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资金
- Light and Efficient Solutions Program (Project SP1) of Finnish Metals and Engineering Competence Cluster (FIMECC Ltd.)
- Finnish Funding Agency for Technology and Innovation (Tekes)
- Rautaruukki Oyj
Using a Gleeble thermomechanical simulator, a high-silicon steel (Fe-0.2C-1.5Si-2.0Mn-0.6Cr) was laboratory hot-rolled, re-austenitized, quenched into the M (s)-M (f) range, retaining 15 to 40 pct austenite at the quench stop temperature (T (Q)), and annealed for 10 to 1000 seconds at or above T (Q) in order to better understand the mechanisms operating during partitioning. Dilatometer measurements, transmission electron microscopy, and calculations showed that besides carbon partitioning, isothermal martensite and bainite form at the partitioning temperature. While isothermal martensite formation starts almost immediately after quenching with the rate of volume expansion dropping all the time, the beginning of bainite formation is marked by a sudden increase in the rate of expansion. The extent of its formation depends on the partitioning temperature following TTT diagram predictions. At the highest partitioning temperatures martensite tempering competes with partitioning. Small fractions of bainite and high-carbon martensite formed on cooling from the partitioning temperature. The average carbon content of the austenite retained at room temperature as determined from XRD measurements was close to the carbon content estimated from the M (s) temperature of the martensite formed during the final cooling.
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